| Literature DB >> 28283901 |
Zahra Ebrahimpour1, Mehdi Bakavoli2, Ali Shiri1, Seyed Mohammad Seyedi1, Tayebe Asghari1, Joel T Mague3.
Abstract
Derivatives of a new heterocyclic system, pyrimido[5,4-e]thiazolo[3,2-a]pyrimidine 3, were prepared by sequential treatment of ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate 1 with 4,5-dihydrothiazol-2-amine 2 and various secondary amines. Single crystal X-ray analysis confirmed the structure of the regioisomer 3. The photophysical characterization of these new compounds was performed by UV/VIS absorption and fluorescence emission spectroscopy. Out of six derivatives studied, only four products 4a-d showed relatively strong fluorescence intensity. The relevant photophysical parameters for all derivatives in this series, including quantum yields and Stokes shifts for the best fluorophores are given.Entities:
Keywords: Fluorescence spectroscopy; Heterocyclization; Pyrimidothiazolopyrimidine; X-ray
Year: 2017 PMID: 28283901 DOI: 10.1007/s10895-017-2055-9
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217